Metabolic engineering of Synechococcus elongatus PCC 7942 for improvement of 1, 3-propanediol and glycerol production based on in silico simulation of metabolic flux distribution. Issue 1 (December 2017)
- Record Type:
- Journal Article
- Title:
- Metabolic engineering of Synechococcus elongatus PCC 7942 for improvement of 1, 3-propanediol and glycerol production based on in silico simulation of metabolic flux distribution. Issue 1 (December 2017)
- Main Title:
- Metabolic engineering of Synechococcus elongatus PCC 7942 for improvement of 1, 3-propanediol and glycerol production based on in silico simulation of metabolic flux distribution
- Authors:
- Hirokawa, Yasutaka
Matsuo, Shingo
Hamada, Hiroyuki
Matsuda, Fumio
Hanai, Taizo - Abstract:
- Abstract Background Production directly from carbon dioxide by engineered cyanobacteria is one of the promising technologies for sustainable future. Previously, we have successfully achieved 1, 3-propanediol (1, 3-PDO) production usingSynechococcus elongatus PCC 7942 with a synthetic metabolic pathway. The strain into which the synthetic metabolic pathway was introduced produced 3.48 mM (0.265 g/L) 1, 3-PDO and 14.3 mM (1.32 g/L) glycerol during 20 days of incubation. In this study, the productivities of 1, 3-PDO were improved by gene disruption selected by screening with in silico simulation. Methods First, a stoichiometric metabolic model was applied to prediction of cellular metabolic flux distribution in a 1, 3-PDO-producing strain ofS. elongatus PCC 7942. A genome-scale model ofS. elongatus PCC 7942 constructed by Knoop was modified by the addition of a synthetic metabolic pathway for 1, 3-PDO production. Next, the metabolic flux distribution predicted by metabolic flux balance analysis (FBA) was used for in silico simulation of gene disruption. As a result of gene disruption simulation, NADPH dehydrogenase 1 (NDH-1) complexes were found by screening to be the most promising candidates for disruption to improve 1, 3-PDO production. The effect of disruption of the gene encoding a subunit of the NDH-1 complex was evaluated in the 1, 3-PDO-producing strain. Results and Conclusions During 20 days of incubation, thendhF1 -null 1, 3-PDO-producing strain showed the highestAbstract Background Production directly from carbon dioxide by engineered cyanobacteria is one of the promising technologies for sustainable future. Previously, we have successfully achieved 1, 3-propanediol (1, 3-PDO) production usingSynechococcus elongatus PCC 7942 with a synthetic metabolic pathway. The strain into which the synthetic metabolic pathway was introduced produced 3.48 mM (0.265 g/L) 1, 3-PDO and 14.3 mM (1.32 g/L) glycerol during 20 days of incubation. In this study, the productivities of 1, 3-PDO were improved by gene disruption selected by screening with in silico simulation. Methods First, a stoichiometric metabolic model was applied to prediction of cellular metabolic flux distribution in a 1, 3-PDO-producing strain ofS. elongatus PCC 7942. A genome-scale model ofS. elongatus PCC 7942 constructed by Knoop was modified by the addition of a synthetic metabolic pathway for 1, 3-PDO production. Next, the metabolic flux distribution predicted by metabolic flux balance analysis (FBA) was used for in silico simulation of gene disruption. As a result of gene disruption simulation, NADPH dehydrogenase 1 (NDH-1) complexes were found by screening to be the most promising candidates for disruption to improve 1, 3-PDO production. The effect of disruption of the gene encoding a subunit of the NDH-1 complex was evaluated in the 1, 3-PDO-producing strain. Results and Conclusions During 20 days of incubation, thendhF1 -null 1, 3-PDO-producing strain showed the highest titers: 4.44 mM (0.338 g/L) 1, 3-PDO and 30.3 mM (2.79 g/L) glycerol. In this study, we successfully improved 1, 3-PDO productivity on the basis of in silico simulation of gene disruption. … (more)
- Is Part Of:
- Microbial cell factories. Volume 16:Issue 1(2017)
- Journal:
- Microbial cell factories
- Issue:
- Volume 16:Issue 1(2017)
- Issue Display:
- Volume 16, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 16
- Issue:
- 1
- Issue Sort Value:
- 2017-0016-0001-0000
- Page Start:
- 1
- Page End:
- 12
- Publication Date:
- 2017-12
- Subjects:
- Cyanobacteria -- Flux balance analysis -- Synthetic metabolic pathway -- 1, 3-Propanediol
Microbial biotechnology -- Periodicals
Recombinant proteins -- Synthesis -- Periodicals
660.62 - Journal URLs:
- http://pubmedcentral.nih.gov/tocrender.fcgi?journal=100 ↗
http://www.biomedcentral.com/1475-2859 ↗
http://www.microbialcellfactories.com/ ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s12934-017-0824-4 ↗
- Languages:
- English
- ISSNs:
- 1475-2859
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11163.xml